Canonical Allele Identifier: CA2580616900

Gene: CNKSR2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.21497850A>G , CM000685.2:g.21497850A>G	GRCh38
NC_000023.10:g.21515968A>G , CM000685.1:g.21515968A>G	GRCh37
NC_000023.9:g.21425889A>G	NCBI36
NG_016266.1:g.128433A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014927.5:c.741+4A>G MANE Select	NP_055742.2:n.741+4A>G
ENST00000379510.5:c.741+4A>G MANE Select	ENSP00000368824.3:n.741+4A>G
NM_001168647.1:c.741+4A>G	NP_001162118.1:n.741+4A>G
NM_001168647.2:c.741+4A>G	NP_001162118.1:n.741+4A>G
NM_001168647.3:c.741+4A>G	NP_001162118.1:n.741+4A>G
NM_001168648.1:c.741+4A>G	NP_001162119.1:n.741+4A>G
NM_001168648.2:c.741+4A>G	NP_001162119.1:n.741+4A>G
NM_001168648.3:c.741+4A>G	NP_001162119.1:n.741+4A>G
NM_001168649.1:c.741+4A>G	NP_001162120.1:n.741+4A>G
NM_001168649.2:c.741+4A>G	NP_001162120.1:n.741+4A>G
NM_001168649.3:c.741+4A>G	NP_001162120.1:n.741+4A>G
NM_001330770.1:c.741+4A>G	NP_001317699.1:n.741+4A>G
NM_001330770.2:c.741+4A>G	NP_001317699.1:n.741+4A>G
NM_001330771.1:c.741+4A>G	NP_001317700.1:n.741+4A>G
NM_001330771.2:c.741+4A>G	NP_001317700.1:n.741+4A>G
NM_001330772.1:c.741+4A>G	NP_001317701.1:n.741+4A>G
NM_001330772.2:c.741+4A>G	NP_001317701.1:n.741+4A>G
NM_001330773.1:c.741+4A>G	NP_001317702.1:n.741+4A>G
NM_001330773.2:c.741+4A>G	NP_001317702.1:n.741+4A>G
NM_014927.3:c.741+4A>G	NP_055742.2:n.741+4A>G
NM_014927.4:c.741+4A>G	NP_055742.2:n.741+4A>G
ENST00000279451.8:c.741+4A>G	ENSP00000279451.4:n.741+4A>G
ENST00000279451.9:c.741+4A>G	ENSP00000279451.5:n.741+4A>G
ENST00000379510.3:c.741+4A>G	ENSP00000368824.3:n.741+4A>G
ENST00000425654.6:c.741+4A>G	ENSP00000397906.2:n.741+4A>G
ENST00000425654.7:c.741+4A>G	ENSP00000397906.2:n.741+4A>G
ENST00000479158.1:n.180+4A>G
ENST00000479158.2:n.594+4A>G
ENST00000485012.2:n.839+4A>G
ENST00000543067.5:c.741+4A>G	ENSP00000444633.1:n.741+4A>G
ENST00000543067.6:c.741+4A>G	ENSP00000444633.1:n.741+4A>G
ENST00000642359.1:c.741+4A>G	ENSP00000496709.1:n.741+4A>G
ENST00000642460.1:n.886+4A>G
ENST00000642501.1:c.57+4A>G	ENSP00000495189.1:n.57+4A>G
ENST00000643171.1:c.741+4A>G	ENSP00000496186.1:n.741+4A>G
ENST00000643220.1:c.741+4A>G	ENSP00000495012.1:n.741+4A>G
ENST00000643313.1:c.53-18635A>G
ENST00000643841.1:c.741+4A>G	ENSP00000494416.1:n.741+4A>G
ENST00000644075.1:n.254+4A>G
ENST00000644095.1:c.741+4A>G	ENSP00000496088.1:n.741+4A>G
ENST00000644295.1:c.741+4A>G	ENSP00000495501.1:n.741+4A>G
ENST00000644585.1:c.741+4A>G	ENSP00000495954.1:n.741+4A>G
ENST00000644789.1:n.3879+4A>G
ENST00000644798.1:c.741+4A>G	ENSP00000494983.1:n.741+4A>G
ENST00000645038.1:n.1255+4A>G
ENST00000645074.1:c.741+4A>G	ENSP00000496573.1:n.741+4A>G
ENST00000645245.1:c.741+4A>G	ENSP00000495695.1:n.741+4A>G
ENST00000645791.1:c.741+4A>G	ENSP00000494906.1:n.741+4A>G
ENST00000646697.1:c.757+4A>G
ENST00000647423.1:n.806+4A>G
ENST00000647532.1:n.811+4A>G
XM_011545471.1:c.741+4A>G	XP_011543773.1:n.741+4A>G
XM_011545471.3:c.741+4A>G	XP_011543773.1:n.741+4A>G
XM_011545472.1:c.741+4A>G	XP_011543774.1:n.741+4A>G
XM_011545472.3:c.741+4A>G	XP_011543774.1:n.741+4A>G
XM_017029358.2:c.741+4A>G	XP_016884847.1:n.741+4A>G